HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → 3-[(3,4-Dichloro-phenyl)-methoxycarbonylmethyl-amino]-propionic Acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 3-(3,4-Dichloro-phenylamino)-propionic Acid tert-butyl ester | HCID 66783246 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-[(3,4-Dichloro-phenyl)-methoxycarbonylmethyl-amino]-propionic Acid tert-butyl ester | HCID 66783134 | 71.4% |
Reaction Conditions
| Temperature | 115 °C |
|---|
Reaction Steps
A neat solution of 8.82 g (30.39 mmol) of 3-(3,4-dichloro-phenylamino)-propionic acid tert-butyl ester, 13.97 ml (151.97 mmol) of methyl bromoacetate and 17.64 ml (151.97 mmol) of 2,6-lutidine was stirred 14 h at 60° C., diluted with 20 ml of CH3CN and heated at 115° C. for 6 h. The reaction was then partitioned between aq. 10% KHSO4 solution and EtOAc (3×). The organic phases were washed with aq. 10% NaCl solution, dried over Na2SO4 evaporated and purified by flash silica gel column (n-heptane:EtOAc 95:5 to 9:1) to yield 7.86 g (71%) of the title compound as an yellow oil. MS: 362.0 (MH+, 2Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138175B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-626201a9e3994591ab0db9102f675838 |
| Source note | uspto-grants-2012_03 |